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Feasibility of the Adapted H-GRASP Feedback Program in the Chronic Phase Post Stroke.

C

Catholic University (KU) of Leuven

Status and phase

Completed
Phase 2
Phase 1

Conditions

Stroke

Treatments

Behavioral: Adapted H-GRASP feedback program

Study type

Interventional

Funder types

Other

Identifiers

NCT05227521
S66123
1153320N (Other Grant/Funding Number)

Details and patient eligibility

About

In a recent cross-sectional study, it was shown that people with a good observed upper limb (UL) motor function but low perceived UL activity show a reduced daily-life UL activity. The investigators will now investigate the feasibility of a phone-monitored home exercise and feedback program for the UL following stroke and the preliminary effects on the perceived UL activity and actual daily-life UL activity for participants with good observed UL motor function but low perceived UL activity in the chronic phase post-stroke.

Enrollment

19 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Voluntary written informed consent of the participant has been obtained prior to any screening procedures
  2. First-ever unilateral, supratentorial stroke, as defined by the American Heart Association/American Stroke Association
  3. Minimum six months after stroke
  4. Living in the community
  5. ≥18 years old
  6. Good observed UL motor function but low perceived UL activity. Good observed UL motor function is defined as a score >50/66 on the Fugl-Meyer Assessment-Upper Extremity (FMA-UE). Low perceived UL activity is defined as a score ≤75/100 on the hand subscale of the Stroke Impact Scale version 3.0 (SIS-Hand).

Exclusion criteria

  1. Other neurological condition than stroke
  2. Musculoskeletal disorder that affects UL use
  3. No informed consent
  4. Participation in an interventional Study with an investigational medicinal product (IMP) or device

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

19 participants in 1 patient group

AH-GRASP feedback intervention group
Experimental group
Description:
All study participants will receive the AH-GRASP feedback intervention.
Treatment:
Behavioral: Adapted H-GRASP feedback program

Trial contacts and locations

1

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Central trial contact

Bea Essers, MSc; Geert Verheyden, Professor

Data sourced from clinicaltrials.gov

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